Issue 49, 2013

Ln[N(SiMe3)2]3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features

Abstract

The first example of rare earth metal-catalyzed cycloaddition of terminal alkynes to azides resulting in the formation of 1,5-disubstituted 1,2,3-triazoles is described. Preliminary studies revealed that the present cycloaddition shows unprecedented mechanistic features involving a tandem anionic cascade cyclization and anti-addition across the C[triple bond, length as m-dash]C triple bond.

Graphical abstract: Ln[N(SiMe3)2]3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features

Supplementary files

Article information

Article type
Communication
Submitted
08 Apr 2013
Accepted
29 Apr 2013
First published
30 Apr 2013

Chem. Commun., 2013,49, 5589-5591

Ln[N(SiMe3)2]3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features

L. Hong, W. Lin, F. Zhang, R. Liu and X. Zhou, Chem. Commun., 2013, 49, 5589 DOI: 10.1039/C3CC42534G

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